Canonical Allele Identifier: CA543041039

Gene: CCR2

Linked Data

• dbSNP Id: rs1450916653
• gnomAD v2: 3-46399015-C-A
• gnomAD v4: 3-46357524-C-A
• MyVariant Identifiers: chr3:g.46399015C>A (hg19) ; chr3:g.46357524C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357524C>A , CM000665.2:g.46357524C>A	GRCh38
NC_000003.11:g.46399015C>A , CM000665.1:g.46399015C>A	GRCh37
NC_000003.10:g.46374019C>A	NCBI36
NG_021428.1:g.8781C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445132.3:c.-4C>A MANE Select	ENSP00000399285.2:n.-4C>A
ENST00000292301.4:c.-4C>A	ENSP00000292301.3:n.-4C>A
ENST00000400888.2:c.-4C>A	ENSP00000383681.2:n.-4C>A
ENST00000421659.1:c.-4C>A	ENSP00000396736.1:n.-4C>A
ENST00000445132.2:c.-4C>A	ENSP00000399285.2:n.-4C>A
ENST00000465202.1:n.315-593C>A
NM_001123041.2:c.-4C>A	NP_001116513.2:n.-4C>A
NM_001123396.1:c.-4C>A	NP_001116868.1:n.-4C>A
XM_011534069.1:c.-4C>A	XP_011532371.1:n.-4C>A
NM_001123396.2:c.-4C>A	NP_001116868.1:n.-4C>A
NM_001123396.3:c.-4C>A	NP_001116868.1:n.-4C>A
NM_001123041.3:c.-4C>A	NP_001116513.2:n.-4C>A
NM_001123396.4:c.-4C>A MANE Select	NP_001116868.1:n.-4C>A